The 3q29 deletion confers >40-fold increase in risk for schizophrenia von Mulle, J G

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Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts von Moreno-De-Luca, D, Sanders, S J, Willsey, A J, Mulle, J G, Lowe, J K, Geschwind, D H, State, M W, Martin, C L, Ledbetter, D H

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Functional evaluation of a PTSD-associated genetic variant: estradiol regulation and ADCYAP1R1 von Mercer, K B, Dias, B, Shafer, D, Maddox, S A, Mulle, J G, Hu, P, Walton, J, Ressler, K J

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A distinct cognitive profile in individuals with 3q29 deletion syndrome von Klaiman, C., White, S. P., Saulnier, C., Murphy, M., Burrell, L., Cubells, J., Walker, E., Mulle, J. G.

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Adaptive behaviour deficits in individuals with 3q29 deletion syndrome von Pollak, R. M., Burrell, T. L., Cubells, J. F., Klaiman, C., Murphy, M. M., Saulnier, C. A., Walker, E. F., White, S. P., Mulle, J. G.

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No evidence for association to the G72/G30 locus in an independent sample of schizophrenia families von Mulle, J G, Chowdari, K V, Nimgaonkar, V, Chakravarti, A

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Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission von Mulle, J G, Fallin, M D, Lasseter, V K, McGrath, J A, Wolyniec, P S, Pulver, A E

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Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders von Mosley, Trenell J, Johnston, H Richard, Cutler, David J, Zwick, Michael E, Mulle, Jennifer G

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The Thanatomicrobiome: A Missing Piece of the Microbial Puzzle of Death von Javan, Gulnaz T, Finley, Sheree J, Abidin, Zain, Mulle, Jennifer G

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Evidence for linkage to chromosome 13q32 in an independent sample of schizophrenia families von Mulle, J G, McDonough, J A, Chowdari, K V, Nimgaonkar, V, Chakravarti, A

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5-Hydroxymethylation-associated epigenetic modifiers of Alzheimer's disease modulate Tau-induced neurotoxicity von Bernstein, Alison I, Lin, Yunting, Street, R Craig, Lin, Li, Dai, Qing, Yu, Li, Bao, Han, Gearing, Marla, Lah, James J, Nelson, Peter T, He, Chuan, Levey, Allan I, Mullé, Jennifer G, Duan, Ranhui, Jin, Peng

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Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects von Rambo-Martin, Benjamin L, Mulle, Jennifer G, Cutler, David J, Bean, Lora J H, Rosser, Tracie C, Dooley, Kenneth J, Cua, Clifford, Capone, George, Maslen, Cheryl L, Reeves, Roger H, Sherman, Stephanie L, Zwick, Michael E

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Bursts of action potential waveforms relieve G-protein inhibition of recombinant P/Q-type Ca2+ channels in HEK 293 cells von Brody, D L, Patil, P G, Mulle, J G, Snutch, T P, Yue, D T

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Functional evaluation of a PTSD-associated genetic variant: estradiol regulation and ADCYAP1R1 von Mercer, K B, Dias, B, Shafer, D, Maddox, S A, Mulle, J G, Hu, P, Walton, J, Ressler, K J

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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities von Kaminsky, Erin B, Kaul, Vineith, Paschall, Justin, Church, Deanna M, Bunke, Brian, Kunig, Dawn, Moreno-De-Luca, Daniel, Moreno-De-Luca, Andres, Mulle, Jennifer G, Warren, Stephen T, Richard, Gabriele, Compton, John G, Fuller, Amy E, Gliem, Troy J, Huang, Shuwen, Collinson, Morag N, Beal, Sarah J, Ackley, Todd, Pickering, Diane L, Golden, Denae M, Aston, Emily, Whitby, Heidi, Shetty, Shashirekha, Rossi, Michael R, Rudd, M Katharine, South, Sarah T, Brothman, Arthur R, Sanger, Warren G, Iyer, Ramaswamy K, Crolla, John A, Thorland, Erik C, Aradhya, Swaroop, Ledbetter, David H, Martin, Christa L

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Inhibition of Recombinant Ca2+ Channels by Benzothiazepines and Phenylalkylamines: Class-Specific Pharmacology and Underlying Molecular Determinants von Cai, Dongming, Mulle, Jennifer G., Yue, David T.

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Plaquettes en « hibernation » : à propos d’un cas von Stockel, G., Thibault, T., Rajillah, A., Hssaini, N. El, Lecluse, J., Turcu, A., Muller, G., Devilliers, H., Auvens, C.

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Editorial overview: Rare CNV disorders and neuropsychiatric phenotypes: opportunities, challenges, solutions von Mulle, Jennifer Gladys, Sullivan, Patrick F, Hjerling-Leffler, Jens

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Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects von Ramachandran, Dhanya, Zeng, Zhen, Locke, Adam E, Mulle, Jennifer G, Bean, Lora J H, Rosser, Tracie C, Dooley, Kenneth J, Cua, Clifford L, Capone, George T, Reeves, Roger H, Maslen, Cheryl L, Cutler, David J, Feingold, Eleanor, Sherman, Stephanie L, Zwick, Michael E

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Critical determinants of Ca(2+)-dependent inactivation within an EF-hand motif of L-type Ca(2+) channels von Peterson, B Z, Lee, J S, Mulle, J G, Wang, Y, de Leon, M, Yue, D T

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